HPLC/GC Expert (Eugene, OR)

ProPharma; Raleigh (NC); Hybrid; USD 83,000 - 124,000; Full time

Job summary

ProPharma is seeking an experienced analytical development specialist to support its synthetic chemistry team on a six-week contract starting mid-September. The focus is on HPLC method development and validation to support small molecule API manufacturing.

The ideal candidate has 7+ years in pharma QC or analytical methods, hands-on HPLC and GC experience, and a collaborative, proactive approach. This role offers hybrid work in the US with potential office collaboration.

Qualifications

• 7+ yrs of experience in small molecule pharma QC or analytical method development.
• Experience with HPLC method development and qualification/validation.

Responsibilities

• Lead analytical development to support the synthetic chemistry team for the next ~6 weeks.
• Develop and qualify/validate HPLC methods for small molecule API manufacturing.

Skills

Analytical method development

Quality control

Team collaboration

Tools

HPLC

GC

Method validation

Job description

For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle.With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs.

This is a six-week contract, beginning in mid-September.

• We’re looking for someone who can help do/lead analytical development to support their synthetic team for the next month and a half.
• This candidate will need to be experienced with both HPLC development of methods to support small molecule API manufacturing and the qualification/validation of those methods.

Requirements:

• 7+ yrs of experience of small molecule pharma QC or analytical method development
• Location: Eugene, OR

#LI-EB3

#API

#AnalyticalMethodDevelopment

#HPLC

#GC

We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.

All applications to roles at ProPharma are personally reviewed by a member of our recruitment team. We do not rely on AI screening tools to support our hiring process. You will always receive an outcome to your application so that you have an answer from us - whether you’re successful or not.

Whilst ProPharma supports remote working, we also recognise the value that comes from in person collaboration. As such, we encourage any new hires that are based within a reasonably short commute of one of our offices to work on a hybrid basis and spend some time working from that office location, as agreed with your manager. All applications will be treated on their own merit and candidates will not be at any advantage or disadvantage based on their proximity to an office.